Evidence map›Paper›PMID 33519911›Full record

ArticleFrontiers in genetics2020

Long Non-coding RNA SNHG17 Upregulates RFX1 by Sponging miR-3180-3p and Promotes Cellular Function in Hepatocellular Carcinoma.

Tao Ma, Xujun Zhou, Hailiang Wei, Shuguang Yan, Yi Hui, Yonggang Liu, Hui Guo, Qian Li, Jingtao Li, Zhanjie Chang and 1 more

Open access · goldAbstract read
In one paragraph

Article in Frontiers in genetics, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 21 papers.

0numbers the graph read from it
0cells of the map it votes in
21citing papers in PubMed
2.3field-weighted citation impact, top 11% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

21 citing papers in PubMed, 29 citations in OpenAlex.

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  9. Long Non-Coding RNAs as "MYC Facilitators".Pathophysiology : the official journal of the International Society for Pathophysiology · 2023
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4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

11 authors at 5 institutions in 1 country.

Tao MaDepartment of Clinical Laboratory, Hospital of Chengdu University of Traditional Chinese Medicine, Chengdu, China.
Xujun ZhouDepartment of Gastroenterology, Wuhan Eighth Hospital, Wuhan, China.
Hailiang WeiDepartment of General Surgery, The Hospital Affiliated to Shaanxi University of Chinese Medicine, Xianyang, China.
Shuguang YanCollege of Basic Medicine, The Shaanxi University of Chinese Medicine, Xianyang, China.
Yi HuiCollege of Basic Medicine, The Shaanxi University of Chinese Medicine, Xianyang, China.
Yonggang LiuDepartment of Liver Diseases, The Hospital Affiliated to Shaanxi University of Chinese Medicine, Xianyang, China.
Hui GuoDepartment of General Surgery, The Hospital Affiliated to Shaanxi University of Chinese Medicine, Xianyang, China.
Qian LiMedical Experiment Center, The Shaanxi University of Chinese Medicine, Xianyang, China.
Jingtao LiDepartment of Liver Diseases, The Hospital Affiliated to Shaanxi University of Chinese Medicine, Xianyang, China.
Zhanjie ChangDepartment of Liver Diseases, The Hospital Affiliated to Shaanxi University of Chinese Medicine, Xianyang, China.
Xiao-Xin MuKey Laboratory of Liver Transplantation, Chinese Academy of Medical Sciences, Nanjing, China.
Shaanxi University of Chinese Medicine · CNAffiliated Hospital of Shaanxi University of Chinese Medicine · CNChengdu University of Traditional Chinese Medicine · CNNanjing Medical University · CNThe Eighth Hospital of Xi'an · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundHepatocellular carcinoma (HCC) is one of the most common types of cancer that is associated with poor quality of life in patients and a global health burden. The mechanisms involved in the development and progression of HCC remain poorly understood.

methodsHepatocellular carcinoma human samples and cell lines were subjected to qRT-PCR for expression assessment. CCK-8 assay, Transwell migration and invasion assay, were applied for cell function detection. Animal experiment was used to measure the function of SNHG17 on cell growth

resultsOur study demonstrated that SNHG17 was upregulated in HCC human samples and involved cell proliferation, migration, invasion progress. SNHG17 promoted HCC cell growth and metastasis

conclusionWe determined RFX1 as the target of miR-3810-3p; SNHG17 enhanced the progression of HCC via the miR-3180-3p/RFX1 axis. Taken together, our findings may provide insight into the molecular mechanism involved in the progression of HCC and develop SNHG17 as a novel therapeutic target against HCC.

Indexed as

hepatocellular carcinomalncRNAmiR-3180-3pRFX1SNHG17

Identifiers

PMID33519911
PMCPMC7844393
OpenAlexW3120120960

What OpenQuestion holds

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Registered trials

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.